Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays (Q24676798)

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English	Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays	scientific article

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scholarly article

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Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays (English)

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single-nucleotide polymorphism

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based on heuristic

inferred from title

object named as

Motohiro Kato

3

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9

object named as

Shigeru Chiba

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author name string

Go Yamamoto

1

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Yasuhito Nannya

2

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Masashi Sanada

4

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Ross L Levine

5

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Norihiko Kawamata

6

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Akira Hangaishi

7

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Mineo Kurokawa

8

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D Gary Gilliland

10

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H Phillip Koeffler

11

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Seishi Ogawa

12

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language of work or name

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publication date

July 2007

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American Journal of Human Genetics

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81

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1

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114-26

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Inferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

7 April 2017

CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

7 April 2017

Two genetic hits (more or less) to cancer

1 reference

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7 April 2017

A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia

1 reference

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7 April 2017

A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

7 April 2017

Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

7 April 2017

A gain-of-function mutation of JAK2 in myeloproliferative disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

7 April 2017

Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

7 April 2017

Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

7 April 2017

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

28 September 2017

PLASQ: a generalized linear model-based procedure to determine allelic dosage in cancer cells from SNP array data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

28 September 2017

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

28 September 2017

Whole genome DNA copy number changes identified by high density oligonucleotide arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

28 September 2017

Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

28 September 2017

An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

28 September 2017

High-resolution analysis of DNA copy number using oligonucleotide microarrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

28 September 2017

Progenitors homozygous for the V617F mutation occur in most patients with polycythemia vera, but not essential thrombocythemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

28 November 2018

Acquisition of the V617F mutation of JAK2 is a late genetic event in a subset of patients with myeloproliferative disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

28 November 2018

Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

28 November 2018

Large-scale genotyping of complex DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1950910

28 November 2018

Exploring polycythaemia vera with fluorescence in situ hybridization: additional cryptic 9p is the most frequent abnormality detected

1 reference

https://pubmed.ncbi.nlm.nih.gov/17564968

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of the recurrent unbalanced translocation der(1;7)(q10;p10)

1 reference

https://pubmed.ncbi.nlm.nih.gov/17564968

12 December 2020

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Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias

1 reference

https://pubmed.ncbi.nlm.nih.gov/17564968

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based on heuristic

inferred from PubMed ID database lookup

Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias

1 reference

https://pubmed.ncbi.nlm.nih.gov/17564968

12 December 2020

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inferred from PubMed ID database lookup

Genome-wide analysis for loss of heterozygosity in primary and recurrent phyllodes tumor and fibroadenoma of breast using single nucleotide polymorphism arrays

1 reference

https://pubmed.ncbi.nlm.nih.gov/17564968

12 December 2020

based on heuristic

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Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays

1 reference

https://pubmed.ncbi.nlm.nih.gov/17564968

12 December 2020

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